Abstract
Ubiquitin-proteasome pathway (UPP) is one of the ways utilized for selective degradation of many proteins in cells, and the 20S proteasome takes the functional machinery where hydrolysis of targeted proteins takes place. Based on existing peptide inhibitors, a series of novel tripeptidic tetrazoles have been designed, synthesized, and the structures have been confirmed with 1H NMR, MS and elemental analysis. Among them, three compounds (6b, 6d and 6h) showed inhibitory activities of ChT-L of 20S proteasome.
Publication types
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English Abstract
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Research Support, Non-U.S. Gov't
MeSH terms
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Biological Assay
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Drug Design*
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Molecular Structure
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Oligopeptides / chemical synthesis*
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Oligopeptides / chemistry
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Oligopeptides / pharmacology
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Proteasome Endopeptidase Complex / chemistry*
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Proteasome Inhibitors / chemical synthesis*
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Proteasome Inhibitors / chemistry
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Proteasome Inhibitors / pharmacology
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Tetrazoles / chemical synthesis*
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Tetrazoles / chemistry
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Tetrazoles / pharmacology
Substances
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Oligopeptides
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Proteasome Inhibitors
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Tetrazoles
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Proteasome Endopeptidase Complex